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Job Description:
Duties & Responsibility:
- Schedule incoming material sampling, identification, and testing activities.
- Verify testing reports to ensure data integrity and compliance with established analytical procedures for raw and packaging material testing.
- Support activities related to alternating or secondary sources of materials in the QC Laboratory.
- Support the preparation and availability of registration documents required from the QC Department.
- Create and revise specifications for packaging materials and raw materials.
- Support the completion of CAPA and CCR action task.
- Support the creation and revision of SOPs, conduct periodic reviews of local SOPs, and perform gap assessments against Global SOPs.
- Manage laboratory operational activities, including Excel spreadsheet control, routine logbook review, periodic backup of QC instruments, and management of reagents and standards.
- Serve as Lead Investigator for laboratory investigations and deviations.
- Contribute to the implementation of energy-saving initiatives within the assigned work area.
- Ensure EHS rules are properly implemented by teams within their respective work areas, in the capacity of EHS Committee Member and Chemical Occupational Health & Safety (OHS) Officer.
- Participate in internal audits as required.
Requirement:
- Associate's degree/ Bachelor of Pharmacist
- Min. 1 year in QC Specialist or or in a closely related position
- Have necessary laboratory skills
- Good English competency (reading, listening and speaking)
- Strong analytical, communication and interpersonal skills
- Proficient in MS Word, Excel and PowerPoint
Locations:
Bekasi, Indonesia
Worker Type:
Employee
Worker Sub-Type:
Fixed Term (Fixed Term)
Time Type:
Full time
